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    NDC 71205-0987-60 Solifenacin Succinate 10 mg/1 Details

    Solifenacin Succinate 10 mg/1

    Solifenacin Succinate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is SOLIFENACIN SUCCINATE.

    Product Information

    NDC 71205-0987
    Product ID 71205-987_b4c66056-a377-4e1a-8708-283ab85b2fb3
    Associated GPIs 54100055200330
    GCN Sequence Number 057983
    GCN Sequence Number Description solifenacin succinate TABLET 10 MG ORAL
    HIC3 R1I
    HIC3 Description URINARY TRACT ANTISPASMODIC, M(3) SELECTIVE ANTAG.
    GCN 23277
    HICL Sequence Number 026595
    HICL Sequence Number Description SOLIFENACIN SUCCINATE
    Brand/Generic Generic
    Proprietary Name Solifenacin Succinate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Solifenacin Succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name SOLIFENACIN SUCCINATE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211657
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0987-60 (71205098760)

    NDC Package Code 71205-987-60
    Billing NDC 71205098760
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-987-60)
    Marketing Start Date 2020-05-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 6e140c11-2b1a-4c3b-9df7-b1b3aa33cfa2 Details

    Revised: 6/2020